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T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea
BACKGROUND: Obstructive sleep apnea (OSA) is a low-grade inflammatory disease affecting the cardiovascular and metabolic systems. Increasing OSA severity reduces T-regulatory lymphocytes (Tregs) in OSA children. Since Tregs modulate endothelial activation, and attenuate insulin resistance, we hypoth...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728363/ https://www.ncbi.nlm.nih.gov/pubmed/23936084 http://dx.doi.org/10.1371/journal.pone.0069710 |
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author | Tan, Hui-Leng Gozal, David Samiei, Arash Bhattacharjee, Rakesh Wang, Yang Ramirez, Helena Molero Bandla, Hari P. R. Kulkarni, Richa Kheirandish-Gozal, Leila |
author_facet | Tan, Hui-Leng Gozal, David Samiei, Arash Bhattacharjee, Rakesh Wang, Yang Ramirez, Helena Molero Bandla, Hari P. R. Kulkarni, Richa Kheirandish-Gozal, Leila |
author_sort | Tan, Hui-Leng |
collection | PubMed |
description | BACKGROUND: Obstructive sleep apnea (OSA) is a low-grade inflammatory disease affecting the cardiovascular and metabolic systems. Increasing OSA severity reduces T-regulatory lymphocytes (Tregs) in OSA children. Since Tregs modulate endothelial activation, and attenuate insulin resistance, we hypothesized that Tregs are associated with endothelial and metabolic dysfunction in pediatric OSA. METHODS: 50 consecutively recruited children (ages 4.8–12 years) underwent overnight polysomnography and fasting homeostatic model (HOMA) of insulin resistance was assessed. Percentage of Tregs using flow cytometry, and endothelial function, expressed as the time to peak occlusive hyperemia (Tmax), were examined. In a subgroup of children (n = 21), in vitro Treg suppression tests were performed. RESULTS: Circulating Tregs were not significantly associated with either BMI z score or HOMA. However, a significant inverse correlation between percentage of Tregs and Tmax emerged (p<0.0001, r = −0.56). A significant negative correlation between Tregs suppression and the sleep pressure score (SPS), a surrogate measure of sleep fragmentation emerged (p = 0.02, r = −0.51) emerged, but was not present with AHI. CONCLUSIONS: Endothelial function, but not insulin resistance, in OSA children is strongly associated with circulating Tregs and their suppressive function, and appears to correlate with sleep fragmentation. Thus, alterations in T cell lymphocytes may contribute to cardiovascular morbidity in pediatric OSA. |
format | Online Article Text |
id | pubmed-3728363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37283632013-08-09 T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea Tan, Hui-Leng Gozal, David Samiei, Arash Bhattacharjee, Rakesh Wang, Yang Ramirez, Helena Molero Bandla, Hari P. R. Kulkarni, Richa Kheirandish-Gozal, Leila PLoS One Research Article BACKGROUND: Obstructive sleep apnea (OSA) is a low-grade inflammatory disease affecting the cardiovascular and metabolic systems. Increasing OSA severity reduces T-regulatory lymphocytes (Tregs) in OSA children. Since Tregs modulate endothelial activation, and attenuate insulin resistance, we hypothesized that Tregs are associated with endothelial and metabolic dysfunction in pediatric OSA. METHODS: 50 consecutively recruited children (ages 4.8–12 years) underwent overnight polysomnography and fasting homeostatic model (HOMA) of insulin resistance was assessed. Percentage of Tregs using flow cytometry, and endothelial function, expressed as the time to peak occlusive hyperemia (Tmax), were examined. In a subgroup of children (n = 21), in vitro Treg suppression tests were performed. RESULTS: Circulating Tregs were not significantly associated with either BMI z score or HOMA. However, a significant inverse correlation between percentage of Tregs and Tmax emerged (p<0.0001, r = −0.56). A significant negative correlation between Tregs suppression and the sleep pressure score (SPS), a surrogate measure of sleep fragmentation emerged (p = 0.02, r = −0.51) emerged, but was not present with AHI. CONCLUSIONS: Endothelial function, but not insulin resistance, in OSA children is strongly associated with circulating Tregs and their suppressive function, and appears to correlate with sleep fragmentation. Thus, alterations in T cell lymphocytes may contribute to cardiovascular morbidity in pediatric OSA. Public Library of Science 2013-07-30 /pmc/articles/PMC3728363/ /pubmed/23936084 http://dx.doi.org/10.1371/journal.pone.0069710 Text en © 2013 Tan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tan, Hui-Leng Gozal, David Samiei, Arash Bhattacharjee, Rakesh Wang, Yang Ramirez, Helena Molero Bandla, Hari P. R. Kulkarni, Richa Kheirandish-Gozal, Leila T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title | T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title_full | T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title_fullStr | T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title_full_unstemmed | T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title_short | T Regulatory Lymphocytes and Endothelial Function in Pediatric Obstructive Sleep Apnea |
title_sort | t regulatory lymphocytes and endothelial function in pediatric obstructive sleep apnea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728363/ https://www.ncbi.nlm.nih.gov/pubmed/23936084 http://dx.doi.org/10.1371/journal.pone.0069710 |
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